Monossacáridos

<p>Sedoheptulose-1-phosphate is a ribosomal metabolite that is produced by marine microorganisms. It is catabolized by sedoheptulose-7-phosphate kinase and converted to the pentose phosphate pathway. The metabolic profile of sedoheptulose-1-phosphate has been shown to be altered in response to environmental stress, such as changes in pH, oxygen levels, and temperature. Sedoheptulose-1-phosphate has also been shown to have structural properties similar to those of ATP and ADP, which may make it an important target for the development of antibiotics.</p>

<p>4,6-O-Benzylidene-D-galactose is an anomer of D-galactose. It is a lectin that has been shown to inhibit the binding of amyloid beta to the cerebroside in the brain tissue. This activity may be due to its ability to form an amide bond with galactose, which is present in amyloid beta. 4,6-O-Benzylidene-D-galactose also has a coronary heart disease prevention effect and can help reduce cholesterol levels. Furthermore, it has been found to have anti-cancer properties and can help prevent the growth of cancerous cells by inhibiting protein synthesis. In addition, 4,6-O-Benzylidene-D-galactose can be used as a cationic surfactant or detergent composition for cleaning or treating surfaces.</p>

<p>Specific, potent and competitive inhibitor of α-L-fucosidase with Ki of 10 nM. In human breast cancer cells, it causes increase of fucosylation on cell surface molecules such as Lewis X antigen (CD15) and CD44 glycoprotein. The 1-deoxyfuconojirimycin treatment increases invasiveness of cancer cells.</p>

<p>2-Keto-D-glucose is a substrate molecule that is used in the study of plant physiology, enzyme kinetics, and metabolic regulation. It has been shown to be an important factor in redox potential and the activation of detoxification enzymes. 2-Keto-D-glucose has also been found to be an important factor in energy metabolism, as it can be converted into pyruvate and acetyl CoA. 2-Keto-D-glucose is a common substrate molecule for many enzymes, including glycolytic enzymes, hexokinase, alcohol dehydrogenase, lactate dehydrogenase, and phosphofructokinase. 2-Keto-D-glucose has also been found to play a role in human blood serum biochemistry by acting as a substrate for erythrocyte D glucose transporter protein and glycerol kinase.</p>

<p>(3S, 4R) -3, 4-Dihydroxy-2-methyl-D-proline is a synthetic monosaccharide. It is an intermediate in the synthesis of (3S, 4R)-3,4-dihydroxy-2-methyl-D-proline and can be used for the production of glycosylated products. This carbohydrate has been synthesized by fluorination followed by methylation and glycosylation. This is a high purity product that can be custom synthesized to meet your needs.</p>

<p>D-Xylonic acid ammonium salt is a synthetic glycosylation agent that is used in the synthesis of oligosaccharides, polysaccharides, and monosaccharides. D-Xylonic acid ammonium salt is also used to modify glycoproteins and proteoglycans for use in the treatment of various diseases. D-Xylonic acid ammonium salt can be synthesized by the fluorination of D-xylose followed by methylation. This agent can be modified through click chemistry or complex carbohydrate modification. It has a high purity and is readily available for purchase.</p>

<p>1,5-Anhydro-2,3,4-tri-O-benzoyl-D-threo-pent-1-enitol is a high purity compound that is synthesized from D-threo pent 1 enitol. It is a sugar that belongs to the category of complex carbohydrates. This product can be custom synthesized and modified according to customer requirements.</p>

<p>6-Chloro-6-deoxy-D-allose is a synthetic sugar that has been fluorinated to produce the 6-chloro-6-deoxy sugar. The product is soluble in water and ethanol, and has a CAS number of 56982-08-3. It can be custom synthesized for customers with high purity and methylated at any position on the sugar chain. This product can be glycosylated or click modified, depending on customer needs.</p>

<p>Ethyl β-D-thioglucopyranoside is a custom synthesis that has been modified with fluorination and methylation, which has made it a monosaccharide. This product is synthetic and can be used for click modification. It is also an oligosaccharide, saccharide, and polysaccharide. Ethyl β-D-thioglucopyranoside is a sugar that belongs to the complex carbohydrate group. It is highly pure and has no impurities.</p>

<p>tert-Butyl b-D-glucopyranoside is a monomer that belongs to the class of acrylic acid ester. It is used in polymer synthesis, as a photoinitiator and as a light stabilizer for polymers. The compound is resistant to heat and has a high degree of light transmittance. Tert-butyl b-D-glucopyranoside is soluble in chloroform and can be found in carbon tetrachloride solution with a transmittance of up to 83%. This compound can be used as an indexing agent for silicon wafers because it produces protrusions when immersed in chloroform.</p>

<p>2,3,4,6-Tetra-O-acetyl-a-D-glucopyranosyl trichloroacetimidate (2TG) is a mannose targeting agent that can be used to target specific cells in the body. This compound has been shown to inhibit the growth of cancer cells and induce photodynamic therapy. 2TG is a conjugate that consists of a 6-phosphate group attached to an acetylated mannose molecule. The 6-phosphate group is an important feature for tumor targeting, as it allows for the attachment of other molecules such as monoclonal antibodies and drugs. 2TG functions by binding with high affinity to glycoproteins on the surface of cancer cells and animal tissues. These glycoproteins are found in large quantities on the surface of cancer cells and animal tissue, which makes them good targets for anti-cancer drug development.</p>

<p>Tetracycline 10-O-b-D-galactopyranoside is a tetracycline antibiotic that has been modified with a fluorinating agent to increase its water solubility. Tetracycline 10-O-b-D-galactopyranoside is the most active of the tetracyclines for the treatment of infections caused by mycoplasmas, rickettsias, and chlamydiae. It inhibits protein synthesis in these bacteria by binding to ribosomes. This drug also has an inhibitory effect on the growth of Mycobacterium tuberculosis and Mycobacterium avium complex.</p>

<p>6-O-Malonylglycitin is a glycosylated flavonoid that belongs to the group of isoflavones. It is found in a variety of plants, including soybeans and fava beans. 6-O-Malonylglycitin has been shown to be an effective inhibitor of β-glucosidase activity at temperatures below 37°C, which overlaps with the range of temperatures where it inhibits glycitein production. This inhibition may be due to its pleiotropic effects on various treatments, such as its ability to inhibit cancer cell growth by inhibiting protein synthesis and inducing apoptosis. 6-O-Malonylglycitin also has synergistic effects when used concomitantly with chromatographic markers, such as high performance liquid chromatography (HPLC), which can be used to analyze the levels of endogenous compounds in human blood samples.</p>

<p>D-Arabonic acid-1,4-lactone is a synthetic sugar that is modified to produce a variety of carbohydrates. This product can be used in the synthesis of oligosaccharides and monosaccharides. It is also used as a carbohydrate in the production of saccharide-based polymers, such as polysaccharides or polyols. This product has CAS number 2782-09-4 and a purity level of ≥99%.</p>

<p>D-Tagatose-6-phosphate barium salt is a custom synthesis, modification, fluorination, methylation, and monosaccharide. It has CAS No. and is a polysaccharide. D-tagatose-6-phosphate barium salt is a complex carbohydrate with glycosylation and sugar.</p>

<p>3-Deoxy-3-fluoro-D-galactitol is a fluorinated sugar that is synthesized through the use of glycosylation and fluorination. This product can be used as a raw material for the production of oligosaccharides, polysaccharides, and other complex carbohydrates. It can also be used in custom synthesis and click modification. The CAS number for this product is 1241800-31-6.</p>

<p>3,5-O-Isopropylidene-D-lyxonic acid gamma-lactone is a sugar that belongs to the group of carbohydrates. It is synthesized by the chemical modification of D-lyxonic acid and has been shown to inhibit the growth of bacteria. 3,5-O-Isopropylidene - D-lyxonic acid gamma-lactone inhibits bacterial growth by binding to the enzyme beta - galactosidase, which is involved in glycosylation and glycosyltransferase activity. This compound also inhibits protein synthesis in bacteria and has been shown to have antiinflammatory properties. 3,5-O-Isopropylidene - D-lyxonic acid gamma-lactone may be used as an alternative sweetener or food additive.</p>

<p>4-Deoxy-4-fluoro-D-glucosamine is a carbohydrate that is used as an inhibitor of the enzyme l1210. This enzyme is required for the biosynthesis of the glycoprotein on the surface of some types of leukemia cells. 4-Deoxy-4-fluoro-D-glucosamine has been shown to be effective in inhibiting leukemia cell growth, and in some cases it has been shown to induce tumor regression. It inhibits protein synthesis by binding to the enzymes responsible for this process.</p>

<p>1-O-Galloyl-b-D-glucose is a molecule that is found in plants and has been used as an inhibitor of p-hydroxybenzoic acid (PHBA) enzyme activities. 1OGG inhibits the growth of viruses by inhibiting the enzymatic activity of their RNA polymerases. It also inhibits mitochondrial membrane potential, which is vital for cellular respiration. 1OGG has shown to be active against urinary infections and opportunistic fungal infections such as Candida glabrata. In vitro assays have shown that it may have anti-inflammatory properties.</p>

<p>Kifunensine is a potent and specific inhibitor of plant and animal α-mannosidase I with IC50 in nanomolar range. It inhibits the enzyme isoforms in Golgi apparatus (GMI) and endoplasmatic reticulum (ERMI). The compound prevents mannose trimming on glycoproteins and shifts the glycoform content from complex to oligomannose type. It's used for the production of recombinant therapeutic glycoproteins with mannose rich N-linked glycans.</p>

<p>Methyl 2,3,4,6-tetra-O-benzyl-D-galactopyranoside is a trisaccharide that binds to the fluorescent chromophore. It has been shown to have strong binding activity and can be used for the labeling of carbohydrates. Methyl 2,3,4,6-tetra-O-benzyl-D-galactopyranoside is also used in assays to detect toxins or as a fluorescent label for polymers. This compound can be synthesized by reacting methyl 4,6-dibenzyloxybenzoate with glucose in methanol.</p>

<p>1,2-Di-O-acetyl-3-azido-3-deoxy-5-O-toluoyl-D-ribofuranose is a synthetic sugar that can be modified to produce oligosaccharides or polysaccharides. It has a CAS number of 120143-22-8 and is composed of a sugar molecule with an acetyl group on the 2' position and toluene sulfonyl group on the 3' position. This modification can be used for glycosylation or methylation reactions. 1,2-Di-O-acetyl -3,4,6,-triaminopyrimidine is also known as fluorinated ribofuranose.</p>

<p>3,6-Anhydro-D-galactose is a monosaccharide of D-galactose where the 3 and 6 positions are cyclised in an ether link. 3,6-Anhydro-D-galactose is found naturally occurring in Rhodophyta (Red Algae) and is a constituent of the sulphated polysaccharide PLS, which has shown anti-inflammation activity and anti-nociceptive effects. In addition, sulphated polysaccharide is capable of inhibiting the in vitro replication of Herpes simplex virus type 1 (HSV-1) and HIV-1.<br>We also offer this product in 10% aqueous solution (MA07897).</p>

<p>Raspberry ketone glucoside is a hydrogenated, isopropyl palmitate fatty acid. It is a dietary supplement that has been shown to inhibit the activity of matrix metalloproteinases, which are enzymes that break down collagen in the skin and lead to wrinkles. Raspberry ketone glucoside also inhibits tyrosinase, an enzyme involved in the production of melanin. As a result, raspberry ketone glucoside has been shown to reduce pigmentation and inhibit UV-induced skin damage. Raspberry ketone glucoside may have an inhibitory effect on fatty acids by inhibiting the synthesis of fatty acids and reducing the number of fat cells in adipose tissue. This compound is also used as a crystallization aid for cellulose and as an organic solvent for food composition.</p>

<p>A toxic glucosamine derivative, widely used for the induction of diabetes in experimental animals. The compound enters the pancreatic β cells in Langerhans islets via glucose transporter GLUT2. It has the ability to alkylate DNA and trigger the production of ROS and nitric oxide, which contribute to DNA and mitochondrial damage. Moreover, streptozocin inhibits N-acetyl-β-D-glucosaminidase and disrupts O-GlcNAc cycling. This molecule has also been used as antimicrobial compound and chemotherapeutic agent for some types of pancreatic cancer.</p>

<p>Please enquire for more information about 6-O-Desmethyl donepezil glucuronide sodium (Mixture of Diastereomers) including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>1,5-Anhydro-2,3,4-tri-O-benzoyl-6-deoxy-D-arabino-hex-1-enitol is a high purity sugar with a click modification. It is a synthetic monosaccharide that is an important building block for complex carbohydrates. This compound can be modified through methylation, glycosylation, and custom synthesis to produce desired compounds. The 1,5 Anhydro 2,3,4 tri O benzoyl 6 deoxy D arabino hex 1 enitol has shown activity against the fluoroquinolone resistant bacteria Staphylococcus aureus and Mycobacterium tuberculosis. It has also been shown to inhibit the growth of cancer cells in vitro and in vivo.</p>

<p>Methyl b-D-thiogalactopyranoside (MTGP) is a cell lysis agent that can be used for diagnostic purposes to measure enzyme activities in cells. It is also used to determine the kinetic of an enzyme reaction, as well as its acid formation. MTGP has been shown to inhibit sugar transport and metabolism by binding to the sugar molecule and preventing it from passing through cellular membranes. This inhibition prevents the accumulation of proton gradients across the membrane, which disrupts ATP production and leads to cell death. MTGP is also an inhibitor of glucose-6-phosphate dehydrogenase (G6PDH), which converts glucose into sorbitol. Sorbitol accumulates intracellularly and leads to cell death by osmotic lysis.</p>

<p>Raloxifene 6-D-glucuronide is a synthetic compound that consists of the sugar raloxifene and the sugar glucuronic acid. It is a complex carbohydrate with a molecular weight of 569. Raloxifene 6-D-glucuronide is soluble in water and insoluble in most organic solvents. The compound has been modified by fluorination, which increases its stability in water, and by click modification. This compound has been shown to inhibit the activity of bacterial enzymes that are responsible for the synthesis of saccharides, such as oligosaccharides and polysaccharides.</p>

<p>D-Lyxonic acid potassium salt is a pentitol that is a stereospecific, aldonic, and nature D-glycosylamine. It can be synthesized by reacting phenylhydrazine with glycolic acid chloride in the presence of catalytic amounts of sodium hydroxide. The yield is about 98%. This compound has been shown to have anti-inflammatory properties when it reacts with hydrogen chloride to form D-lyxonic acid chloride. It also has been shown to inhibit the growth of bacteria and fungi by binding to the cell wall and inhibiting protein synthesis.</p>

<p>D-Galacturonic acid (GalA) is a hexuronic acid with the CH2OH at C5 of galactose replaced by a carboxyl group (Collins, 2006). D-galacturonic acid is abundant in pectic polysaccharides which are characterized by a high α-1,4 linked galacturonic acid content and include pectic acid (polygalacturonic acid), rhamnogalacturonan I (Oomen, 2002), rhamnogalacturonan (RG) II (Vidal, 2000), xylogalacturonan, and homogalacturonan. These polymers play roles in strengthening cell walls, cell adhesion and are established as part of signaling cascades that detect cell wall degradation upon pathogen attack.</p>

<p>a-D-Glucopyranosyl fluoride is an irreversible inhibitor of the enzyme glycosidase. This product has been used to study the kinetic and mechanism of human serum alpha-glucosidase, which is a key enzyme in the digestion of carbohydrates. Kinetic studies have shown that 4-hydroxycinnamic acid and glucose are competitive inhibitors of the enzyme. The reaction mechanism for this product involves hydrogen fluoride cleavage of the glycosidic bond. The optimum pH for this product is 7.</p>

<p>3,4-Di-O-acetyl-L-fucal is a phosphate derivative that is synthetically derived from ethyl diazoacetate. It has cytotoxic properties and is readily activated by phosphorylation to form the active form. 3,4-Di-O-acetyl-L-fucal has been shown to be effective against leukemia cells in vitro and may be useful as an adjuvant treatment for lymphocytic leukemia. 3,4-Di-O-acetyl-L-fucal also inhibits the growth of staphylococci in vitro, but it is not active against other bacteria such as Escherichia coli or Pseudomonas aeruginosa. The enantiomer of 3,4 Di O acetyl - L - fucal is inactive because it cannot be phosphorylated.</p>

<p>Glucose (Glu) is the most common carbohydrate on the planet, found in all living organisms and is the major source of metabolic energy for plants and animals. Glucose is a building block in numerous oligosaccharides and polysaccharides. It is present in blood and milk, in gangliosides and in N- and O-linked glycans (Collins, 2006). Glucose is wrongly called a simple sugar because in solution it exists in five forms: two six membered rings (α/β), two five membered rings (α/β) and a straight chain form, a system known as mutarotation (Robyt, 2012). The proportions of different glucose forms are dictated by temperature and pH. D-Glucose is optically active (dextrorotary) and L-Glucose is its enantiomer (Levorotary). Its hydroxyl groups are all equatorial, providing maximum stability, according to Hudsons rules (Hudson, 1948).</p>

<p>Galactose from plant origin, animal free production</p>

<p>2,3,5-Tri-O-benzyl-L-xylofuranose is a sugar molecule that has been modified to inhibit glycosidases. 2,3,5-Tri-O-benzyl-L-xylofuranose is an iminosugar that inhibits the enzyme β-glucosidase and α-galactosidase. The compound is not metabolized and it binds to the enzyme's active site. 2,3,5-Tri-O-benzyl L xylofuranose has been shown to be effective at inhibiting all of the glycosidases tested in this study with inhibition potencies ranging from 0.1 mM to 10 mM. This compound also inhibits epoxides and cyclic enzymes such as azido reductase and dihydropyrimidine dehydrogenase.</p>

<p>N-acetylneuraminic acid derivative and a useful tool for the study of sialic acid binding to its ligands. It was previously used for such purpose in studies on the influenza binding to hemagglutinin. This compound was also used for investigation of Clostridium botulinum toxin binding to various sugars.</p>

<p>1,3,4,6-Tetra-O-acetyl-2-deoxy-2-fluoro-D-galactopyranose is a fluorinated sugar that is used in the synthesis of glycosides. It is a synthetic compound that is prepared by reacting 1,3,4,6-tetraacetyl galactose with potassium bifluoride and diethyl oxalate in presence of anhydrous sodium sulfate. The product obtained has the following structural formula: The chemical name for this compound is 1,3,4,6-Tetraacetyl -2-[(1R)-1-(ethoxycarbonyl)propyl]-2-(fluorooxymethyl) -D-galactopyranose. The CAS number for this compound is 83697–45–4.</p>

<p>Phenyl b-L-thiofucopyranoside is a custom-synthesized, fluorinated, modified sugar that is used in the synthesis of oligosaccharides and polysaccharides. This compound is an excellent choice for methylation reactions due to its high reactivity and stability under harsh conditions. Phenyl b-L-thiofucopyranoside can be used as a precursor for the synthesis of saccharide derivatives, such as monosaccharides and complex carbohydrates. It has been shown to be stable to heat and pH extremes, making it ideal for use in organic syntheses.</p>

<p>Emodin is a natural product that can be extracted from the rhizome of Curcuma aromatica, a chinese herb. It has been shown to have neuroprotective effects in animal studies and has been used as an adjuvant in the treatment of cervical cancer. Emodin also inhibits the replication of human immunodeficiency virus type 1 (HIV-1) and herpes simplex virus type 1 (HSV-1). Emodin is also active against microbial infection, including bacterial infections, such as those caused by Staphylococcus aureus, and viral infections, such as influenza A virus. The main mechanism of action of emodin is its inhibition of DNA synthesis by binding to viral dna or bacterial rna polymerase. Emodin has also been found to inhibit protein synthesis by binding to ribosomes. This drug binds to urea nitrogen molecules in bacteria and disrupts their growth by inhibiting protein synthesis.</p>

<p>Substrate for arabitol dehydrogenase enzyme</p>

<p>3-Deoxy-3-fluoro-D-allose is a chemical compound with the molecular formula CHNO. It has been shown to have potential as a contrast agent for magnetic resonance imaging (MRI) and positron emission tomography (PET). The conformation of 3-Deoxy-3-fluoro-D-allose is similar to that of glucose, but it does not inhibit the uptake of glucose by erythrocytes or the transport of glucose across cell membranes. 3DFA has been shown to be taken up by cells in the brain, kidney, and liver. The uptake and distribution of 3DFA in these tissues was dependent on serum protein concentrations.</p>

<p>1,4-Anhydro-D-erythritol is a sugar alcohol that can be found in various plants and fruits. It is a reaction product of D-erythrose and glycerol, with an average formation rate of 10%. The hydroxyl group on the 1,4-anhydro-D-erythritol molecule reacts with methyl glycosides to produce an ester. Trifluoromethanesulfonic acid is used as a catalyst in this process, which activates the hydroxyl group on the molecule. The reaction mechanism for this process involves three steps: elimination of water, dehydration of the hydroxyl group, and addition of methyl glycoside. This process results in a new molecule called 1,4-anhydro-D-erythritol methyl ester (AEME). AEME has been shown to have conformational properties that are different from those of its parent compound. The conformational</p>

<p>L-Glucurono-3,6-lactone is an acetonide that is a derivative of L-glucose. L-Glucurono-3,6-lactone can be used as a precursor for the synthesis of polyhydroxybutyrate (PHB).</p>

<p>D-Xylose-5-phosphate disodium salt is a Custom synthesis that has been fluorinated, methylated, and modified with a click reaction. D-Xylose-5-phosphate disodium salt is also an oligosaccharide and polysaccharide. The CAS No. for this compound is 1083083-57-1.</p>

<p>D-Salicin is a naturally occurring compound, classified as a biologically active glycoside. It is acquired from the bark of willow trees, primarily species within the genus Salix. The primary mode of action of D-Salicin involves its metabolic conversion into salicylic acid within the human body. This conversion occurs in the gastrointestinal tract and bloodstream, ultimately displaying effects similar to non-steroidal anti-inflammatory drugs (NSAIDs).</p>

<p>4-Methoxyphenyl 2-deoxy-3-benzyl-4,6-O-(4-methoxybenzylidene)-2-phthalimido-b-D-glucopyranoside is a custom synthesis that has been modified with fluorination and carbamoylation. This product is an oligosaccharide that belongs to the group of polysaccharides. It is a complex carbohydrate that has been synthesized from monosaccharides and sugar. 4MPBGP is soluble in water and has high purity levels.<br>*The following content was automatically generated by eCommerce software:</p>

<p>Resource for the 6-O-modification of Glc e.g. in glucuronic acid synthesis</p>

<p>2-O-b-D-glucopyranosylcucurbitacin E is a natural product that has been isolated from the roots of Cucurbita maxima. This compound has been shown to have bioactive properties, including antioxidant and antimicrobial activity. The extract was tested on chronic cough patients with type 2 diabetes mellitus. The treatment group showed significant improvements in symptoms and bioactive phytochemical levels compared to the control group.<br>2-O-b-D-glucopyranosylcucurbitacin E is a white powder that is soluble in methanol and water but not in chloroform or ether. It can be analyzed by liquid chromatography, which separates the different components of a sample by passing it through a column filled with an adsorbent material that retains some components more than others.</p>

<p>Salicylic acid-acyl-b-D-glucuronide is an anti-inflammatory compound that is found in the urine of diabetic patients. It has been shown to inhibit the production of a number of proinflammatory compounds, including prostaglandin E2 (PGE2), in human serum. Salicylic acid-acyl-b-D-glucuronide is formed by the reaction of salicylic acid with acetylsalicylic acid. The rate of formation is dependent on the concentration of salicylic acid and pH. The reactive product can form covalent adducts with tyrosinase and other proteins, leading to inhibition of tyrosinase activity and melanin synthesis.</p>

<p>Voglibose is a competitive inhibitor of α-glucosidase used for the control of blood sugar levels in patients with type 2 diabetes mellitus. The compound binds reversibly to intestinal carbohydrate-active digestive enzymes with α-glucosidase activity, inhibits breakdown of complex sugars and consequently delays the absorption of glucose into blood.</p>

<p>L-Xylonic acid-1,4-lactone is an enzyme that functions as a glycolytic enzyme. It catalyzes the conversion of D-xylose to L-xylonic acid and L-xylonic acid-1,4-lactone. This enzyme is expressed in leukemia HL60 cells and is activated by acidic conditions. L-Xylonic acid-1,4-lactone has been shown to be catabolized by the enzyme xylanase. The kinetic properties of this reaction have been studied using mass spectrometric techniques and biochemical methods. The rate of the reaction was found to be dependent on the presence of divalent cations (Mg2+ or Ca2+) or monovalent ions (Na+ or K+). L-Xylonic acid 1,4 lactone also catabolizes glucose with a similar rate constant.</p>

<p>3,4-Di-O-acetyl-L-arabinal is a synthetic compound that belongs to the class of monofluorides. It has been synthesized from l-arabinose by a stereoselective process, with triflic acid as the catalyst and propargylation as the key step. The synthetic pathway starts from an acid hydrolysis of L-arabinose to yield 3,4-di-O-acetyl-L-arabinonic acid. This acid is then converted to 3,4 diacetyl L arabinonic acid with acetic anhydride and acetic acid in the presence of triethylamine. The final product is then obtained by reacting this intermediate with 1 equivalent of sodium fluoride in tetrahydrofuran (THF) using catalytic reduction with sodium borohydride at 0 °C. The major advantage of this synthetic process is that it provides two stereoisomers: (</p>

<p>1,2-Dideoxy-3,5-di-O-toluoyl-D-ribose is a synthetic sugar that can be used in the synthesis of complex carbohydrates. It has been modified with fluorine, methylation, and click chemistry. It is also available as a high purity product. 1,2-Dideoxy-3,5-di-O-toluoyl-D-ribose is an oligosaccharide that is used in glycosylation reactions to form polysaccharides or saccharides. Click chemistry allows for the modification of this sugar with other molecules such as amino acids or peptides. This modification may be useful for studying protein interactions or for drug development.</p>

<p>2,3,4,6-Tetra-O-acetyl-β-D-galactopyranosyl azide is a catalyst that has been used in the production of carbonate catalysts. It can also be used to reoxidize metallic catalysts.</p>

<p>3-Epialexine is a novel small molecule that inhibits sucrase, the enzyme responsible for cleaving glucose from sucrose. 3-Epialexine binds to the active site of this enzyme, preventing d-glucose from binding and being broken down. This leads to an accumulation of d-glucose in the intestinal lumen and could be used as a lead compound for the development of drugs to treat diabetes. The diversity of microorganisms can be screened for sucrase activity by using 3-epialexine as a lead compound.</p>

<p>Phenyl a-D-galactopyranoside is a pesticide that is used to control the growth of endophytic fungi. It has been shown to have an antibacterial effect against Gram-positive bacteria and can be used as a fungicide. Phenyl a-D-galactopyranoside can be synthesized from the corresponding synthons, which are 3-hydroxybenzoic acid and 4-methylphenol. This compound contains a carbonyl group and hydroxyl group that are reactive with enzymes such as esterases, glucuronidases, and glutathione reductase, which hydrolyzes it into its inactive form.</p>

<p>Simvastatin acyl-b-D-glucuronide is a synthetic compound that is not naturally occurring. It has a molecular weight of 571.67 and the CAS number 463962-56-3. The chemical formula for this compound is C30H44O8 and its structural formula is shown below. The purity of this product is &gt;99% and it has been modified with fluorination to improve solubility in water.</p>

<p>Please enquire for more information about 2-Acetamido-2-deoxy-a-D-thiogalactopyranose including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>Phenylethyl-beta-D-glucopyranoside is a phenolic compound that is found in plants such as Echinacea. Phenylethyl-beta-D-glucopyranoside has been shown to inhibit tumor cell proliferation by increasing the levels of enzyme catalysis and enzyme activity, and decreasing the levels of protocatechuic acid. This compound also inhibits fatty acid synthesis, which may be due to its ability to inhibit the production of 4-hydroxycinnamic acid via inhibition of the enzyme acyl coenzyme A:cholesterol acyltransferase. The cyanobacterial strain Synechococcus elongatus PCC 7942 was found to produce phenylethyl glucoside, an iridoid glucoside with high cytotoxic activity against human tumor cells.</p>

<p>2,4-Methanoglutamic acid is an amino acid that has been shown to have neuroprotective effects in animal models of excitotoxicity. It has been shown to reduce neuronal death at low concentrations and inhibit the uptake of glutamate into the brain cells. 2,4-Methanoglutamic acid binds to calcium ions and prevents the release of calcium from intracellular stores, thereby protecting against neuronal death. This compound has also been shown to be toxic in mammalian cell culture, but it is not yet known if this toxicity will occur in humans.</p>

<p>D-Threonic acid-1,4,-lactone is a methylated saccharide that is prepared by the oxidation of D-threo-aldose. It can be used as a building block in the synthesis of glycosylates, oligosaccharides, and polysaccharides. The compound has been shown to inhibit the growth of Mycobacterium tuberculosis and Mycobacterium avium complex. D-Threonic acid-1,4,-lactone can also be fluorinated for use as an imaging agent for positron emission tomography (PET).</p>

<p>Telmisartan acyl-b-D-glucuronide is a drug metabolite that is formed by the conjugation of telmisartan with glucuronic acid. Telmisartan acyl-b-D-glucuronide is activated in vivo and reversibly inhibits the enzyme creatine kinase, which is involved in the metabolism of creatine to creatinine. The effective dose for this compound has been shown to be 10 mg/kg (orally) in humans. Telmisartan acyl-b-D-glucuronide has been shown to be an at1 receptor antagonist and may have some antihypertensive effects via modulation of ion channels. This drug also appears to have some proliferative effects on cells that are inhibited by radiation.</p>

<p>Methyl β-L-arabinopyranoside is a stereochemically pure monosaccharide that has been used to calibrate and quantify the conformational, stereochemical, and spectrometric methods. Methyl β-L-arabinopyranoside has a conformation that is restricted by the presence of an α-hydroxyl group at C2. The chloride ion can be used to monitor this conformation. The diameter of methyl β-L-arabinopyranoside can be measured with a micropipette and monitored using an aerosol detector. Methyl β-L-arabinopyranoside can also be quantified by mass spectrometry or spectrophotometry. The conformational, stereochemical, and spectrometric methods have been calibrated using methyl β-L-arabinopyranoside as a standard to determine their accuracy in measuring the size of other molecules.</p>

<p>D-Glucosamine-oxime HCl is a hydrocyanic acid derivative that contains a polyhydroxy group. It can exist as two isomers, D-glucosamine and D-glucosamine-oxime. These isomers are distinguished by the presence or absence of acetyl groups on the nitrogen atoms. D-Glucosamine-oxime HCl functions as a divalent metal ion chelator and sequestering agent that has been shown to be useful in the treatment of lead poisoning. It also has been used in the synthesis of hydrocyanic acid, which is an important chemical for organic synthesis.END&gt;</p>

<p>Methyl 2-deoxy-3,5-di-O-toluoyl-L-ribofuranoside is a custom synthesis that is a complex carbohydrate that is used in the modification of saccharides. It has been shown to be able to methylate and glycosylate carbohydrates and can be fluorinated for use in click chemistry experiments. Methyl 2-deoxy-3,5-di-O-toluoyl-L-ribofuranoside is highly pure and can be synthesized with high yield.</p>

<p>D-Allono-1,4-lactone is a biochemical compound that has been shown to have immunosuppressant properties. D-Allono-1,4-lactone is an inhibitor of maltase, an enzyme involved in the digestion of starch and glycogen. D-Allono-1,4-lactone also inhibits transglucosylase, an enzyme involved in the conversion of sucrose into glucose. It binds to sulfur transfer proteins and has been shown to be effective against mutants with altered biochemical properties.</p>

<p>Popular resource for chiral-pool based organic syntheses<br>Sold as an aqueous solution and by weight of active material</p>

<p>D-Glucosamine-2-N-sulfate sodium is a synthetic, high purity carbohydrate with a custom synthesis. It is an oligosaccharide that is also a sugar and a saccharide. The methylation of D-glucosamine 2-N-sulfate sodium can be achieved by glycosylation or click modification. Click modification is the addition of a carbon atom to the molecule through the reaction with an electrophile, such as N-hydroxysuccinimide ester. This modification can be used to introduce fluorine atoms into the molecules, which can improve their solubility and stability. The product has shown anti-inflammatory activities in animal models, which may be due to its ability to inhibit prostaglandin synthesis.</p>

<p>Please enquire for more information about 9,10-Anhydro doxorubicin including the price, delivery time and more detailed product information at the technical inquiry form on this page</p>

<p>2,3:4,5-Di-O-isopropylidene-D-xylitol is an acceptor for the Stannic Chloride Reaction. It is a lacto-n-biose derivative of D-xylitol that has been shown to have antibiotic activity against Streptococcus section A and B. The temporary protection of the hydroxyl group in 2,3:4,5diOisopropylidene-Dxylitol with methyl glycosides provides a convenient method for glycosylations. The chloride ion can be replaced by hexaacetate to yield 1amino1deoxyDxylitol hydrochloride, which is a benzyl derivative. This reaction allows for research into the transfer of 2,3:4,5diOisopropylideneDxylitol.</p>

<p>D-Glucose - monohydrate is a glucose molecule that is found in the blood stream. It is the preferred source of energy for the brain and has been shown to enhance brain function. Glucose is also used to maintain the water balance of cells and tissues, as well as to prevent or treat hypoglycemia. This molecule can be found in many foods, such as honey, corn syrup, molasses, fruits and fruit juices. D-Glucose - monohydrate has antibacterial efficacy against a number of bacteria including staphylococcus aureus, Escherichia coli, Pseudomonas aeruginosa and Bacillus subtilis. It can also inhibit squamous cell carcinoma growth in vivo by preventing the proliferation of cancer cells. D-Glucose - monohydrate is structurally similar to adenosine diphosphate (ADP), which binds to dinucleotide phosphate (DP) enzymes that are involved in energy metabolism</p>

<p>Sorbitol hexaacetate is a low-energy compound that has a hydroxyl group and a phenolic acid. It is used as an intermediate in the production of detergents, surfactants, and other industrial chemicals. In addition to this, sorbitol hexaacetate can be used as a radiation shield and an effective dose for radiation therapy. Sorbitol hexaacetate is also used as an ingredient in lipolytic enzymes. It has been shown to inhibit the activity of lipolytic enzymes by forming hydrogen bonds with the enzyme active site. Magnetic resonance spectroscopy studies have revealed that sorbitol hexaacetate has a cavity that can be filled with water molecules, which may explain its ability to act as an optical polarizer.</p>

<p>Methyl 2,3:4,6-di-O-isopropylidene-D-mannopyranoside is a synthetic glycosylate sugar that has been modified with fluorination. It is a monosaccharide that is used in the synthesis of complex carbohydrates. Click modification of this molecule has been performed to yield high purity and desired modifications. CAS number 50705-56-1.</p>

<p>Component of plant, especially grape, glucuronoxylans</p>

<p>3-O-Benzyl-4,6-O-benzylidene-a-D-glucopyranose is a custom synthesis of a complex carbohydrate. This product has CAS No. and can be found under Polysaccharide in the listing of Modified saccharides. It is modified by Methylation, Glycosylation, Click modification and Carbohydrate. The product is synthesized using Fluorination and Synthetic methods. It is high purity, with a purity level of 99%.</p>

<p>D-[5-2H]Glucose is a deuterated form of glucose that is used in the study of lipid synthesis. This isotopically labeled compound can be incorporated into cellular lipids and their derivatives, such as glycerides and phospholipids. D-[5-2H]Glucose can be used to investigate the biosynthesis of lipids by measuring the incorporation rate and the number of 2H atoms found in each molecule. D-[5-2H]Glucose may also be used to study membrane lipid synthesis, which includes anomeric effects on lipid synthesis. The theory behind this is that when a molecule is incorporated into a lipid, it will have at least one hydrogen atom from deuterium instead of hydrogen. This isotopically labeled compound can be used to measure how anomeric effects influence lipid synthesis.</p>

<p>1,2,3,4-Tetra-O-pivaloyl-6-O-triisopropylsilyl-a-D-mannopyranose is a glycosylation product that can be used as a model for the synthesis of complex carbohydrates. It is synthesized by reacting 1,2,3,4 tetra O pivaloyl a D mannopyranose with triisopropyl silyl chloride in the presence of DMAP and 4-(N,N dimethylamino)pyridine. This product can be used to study the methylation of saccharides. The fluorination and saccharide modification are performed using potassium fluoride or potassium chlorate respectively. This product is also available in custom synthesis quantities at high purity.</p>

<p>Important bioactive principle in established anti-inflammatory herbal medicines</p>

<p>7-Azido-7-deoxy-2,3:5,6-di-O-isopropylidene-D-glycero-D-alloheptono-1,4lactone is a methylation product of saccharide and polysaccharides. It is a modification of the natural molecule with an azide group. It has CAS number 47927–03–9. 7A7DL can be modified to produce oligosaccharides or glycosylations with high purity and custom synthesis. It can be fluorinated to produce complex carbohydrates.</p>

<p>4-Methoxyphenyl 6-azido-2,3,4-tri-O-benzyl-6-deoxy-a-D-mannopyranoside is a synthetic sugar molecule that has been modified to contain a benzyl ether moiety. This product can be custom synthesized and is available in high purity.</p>

<p>1,4-Anhydro-6-chloro-6-deoxy-D-glucitol is a complex carbohydrate that has been fluorinated and modified with methyl groups. It can be custom synthesized to produce high purity compounds. 1,4-Anhydro-6-chloro-6-deoxy-D-glucitol is used in synthesis of saccharides and oligosaccharides. The compound has been modified with Click chemistry to produce glycosylation products. It can also be used as an intermediate for the synthesis of sugar derivatives.<br>1,4-Anhydro-6-chloro-6-deoxy--D--glucitol has the following chemical structure:</p>

<p>Methyl 5-Acetamido-N-benzyl-5,6-dideoxy-2,6-imino-3-O-benzyl-L-galactofuranoside is a modified carbohydrate with a methyl group at the C5 position. It is synthesized by modification of the saccharide and has a CAS number. This compound is used as a custom synthesis for synthesis of complex carbohydrates.</p>

<p>2-Deoxy-2-fluoro-D-glucose 6-phosphate barium salt is a glucose analogue used in positron emission tomography (PET) imaging of cancer. It is an inhibitor of glycolysis and phosphofructokinase, which are enzymes that catalyze the conversion of glucose to pyruvate. 2-Deoxy-2-fluoro-D-glucose 6-phosphate barium salt is taken up by the cell by active transport, then metabolized into 2 deoxy 2 fluoro D mannose phosphate and finally converted to glucosylceramide. The PET scan detects the accumulation of this molecule in cells with high glycolytic activity, such as cancer cells. This compound has been shown to inhibit hepatocellular carcinoma (HCC) cell growth in vitro and in vivo.</p>

<p>3-Azido-3-deoxy-5, 6-O-isopropylidene-Dgulonic acid g-lactone is a fluorinated monosaccharide. It is synthesized by the reaction between 3,4,6,7 tetra fluorobenzaldehyde and 5,6 O isopropylidene Dgulonic acid. It can be used for glycosylation reactions in order to produce oligosaccharides. The modification of this product can be achieved through methylation and sugar modification techniques. This product has CAS No. 244057-17-8 and is highly pure with a purity of 99%.</p>

<p>Octahydro-1,2,9-tris-acetoxy-(1S,2R,9S,9aS)-quinolizin-6-one is an oligosaccharide that is a sugar modified with fluorine. It is a synthetic carbohydrate and has the CAS number 57714-00-3. The molecular weight of this compound is 784.61 g/mol. This compound can be custom synthesized to meet your needs and specifications. It has been methylated and glycosylated and has undergone click chemistry modifications.</p>

<p>A solar thermal collector is a device that absorbs the sun's heat, or thermal energy, and converts it to useful heat energy. It consists of a dark-colored surface (usually metal) that absorbs sunlight and transfers the heat by radiation to a fluid such as water or oil, which then carries the heat away for use. The efficiency of this type of collector depends on the quantity of sunlight that reaches it, the temperature difference between the hot fluid and ambient air, and its design. A typical solar thermal collector has an efficiency of about 10%.</p>

<p>Fucose (Fuc, 6-deoxy L-galactose) has a methyl group at C6 in place of a hydroxyl group and this gives the molecule a greater degree of hydrophobicity than galactose (Collins, 2006). L-fucose is found in fucoidan, a polysaccharide that occurs in the brown seaweeds (Phaeophyceae) (Percival, 1967). Fucose is also a key component in many mammalian N- and O-linked glycans, glycolipids, blood group substances and Lewis antigens (Becker, 2003). In human milk, neutral (fucosylated) oligosaccharides (HMO) contain fucose at the terminal position (e.g. 2’ -fucosyllactose and lactodifucopentaose). They represent 35% to 50% of the total HMO content and many in vitro studies suggest that HMOs directly modulate immune responses, acting either locally on cells of the mucosa-associated lymphoid tissues or systemically to inhibit the expression of inflammatory genes, mainly cytokines (Plaza-Diaz, 2018).</p>

<p>5,6-O-Isopropylidene-3-C-methyl-D-mannono-1.4-lactone is a fluorinated monosaccharide that can be modified with other chemicals to create a variety of products. This chemical is used in the synthesis of oligosaccharides and polysaccharides. 5,6-O-Isopropylidene-3-C-methyl-D-mannono-1.4-lactone has a CAS number of 105853-. It has been shown to be high purity and is also available for custom synthesis. 5,6--O--isopropylidene--3--C--methyl--D--mannono--1.4--lactone can be synthesized from methylation, click modification, and fluorination reactions on glycolaldehyde.</p>

<p>5-O-Allyl-2,3,4-tri-O-benzyl-D-ribitol is an acid that has been used in preparative organic chemistry. It is a benzyloxymethyl derivative of ribose, which can be converted to the corresponding methyl ether by hydrolysis with sodium methoxide in methanol. 5-O-Allyl-2,3,4-tri-O-benzyl-D-ribitol functions as an isomer and dimerization reagent for the preparation of propenyl derivatives. 5-O-Allyl 2,3,4 tri O benzyl D ribitol has been shown to inhibit Influenza A H1N1 strains in vitro with a 50% inhibitory concentration (IC50) of 1 μM.</p>